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Dive into the research topics where George F. Huhn is active.

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Featured researches published by George F. Huhn.


Synthetic Communications | 1993

A Large Scale Preparation of the Cognitive Enhancer Linopirdine

Walter M. Bryant; George F. Huhn; James H. Jensen; Michael E. Pierce; C. Stammbach

Abstract Linopirdine is a pharmacologically potent drug which stimulates central nervous system neurotransmitter release. A facile process used to synthesize linopirdine on a commercial manufacturing scale consisting of seven chemical steps with only a single isolated intermediate is described.


Synthetic Communications | 1995

A Practical Preparation of 7-Methoxy-3(2H)-Benzofuranone

Walter M. Bryant; George F. Huhn

Abstract A practical new synthesis suitable for large-scale production of 7-methoxy-3(2H)-benzofuranone by conversion of commercially available 2-hydroxy-3-methoxybenzoic acid to 7-methoxy-3-acetoxybenzofuran followed by hydrolysis is described.


Separation Science and Technology | 1993

Purification of Nucleoside-5′-diphosphates: A New Ion-Exchange Method

George F. Huhn; James H. Jensen; Michael E. Pierce; E. M. Schlabach

Abstract Inosine- and uridine-5′-diphosphates can be purified by ion-exchange chromatography utilizing a new ion-exchange method where Type 1 ion-exchange resins and the absorbed nucleoside polyphosphates are changed to the basic form by rinsing the column with dilute sodium hydroxide and subsequently eluting with dilute hydrochloric acid and sodium chloride.


Journal of Organic Chemistry | 1984

Acid-catalyzed nitronate cycloaddition reactions. Useful syntheses and simple transformations of 3-acyl- and 3-alkenylisoxazolines

Peter A. Wade; Nayan V. Amin; Hwa Kwo Yen; David T. Price; George F. Huhn


Journal of Organic Chemistry | 1993

Practical synthesis and regioselective alkylation of methyl 4(5)-(pentafluoroethyl)-2-propylimidazole-5(4)-carboxylate to give DuP 532, a potent angiotensin II antagonist

Michael E. Pierce; David John Carini; George F. Huhn; Gregory J. Wells; John F. Arnett


Journal of Organic Chemistry | 2000

Efficient Pyridinylmethyl Functionalization: Synthesis of 10,10-Bis[(2-fluoro-4-pyridinyl)methyl]-9(10H)-anthracenone (DMP 543), an Acetylcholine Release Enhancing Agent†

Jaan A. Pesti; George F. Huhn; Jianguo Yin; and Yide Xing; Joseph M. Fortunak; Richard A. Earl


Archive | 1988

Process for preparing 3,3-disubstituted indolines

Walter M. Bryant; George F. Huhn


Journal of Heterocyclic Chemistry | 1998

Synthesis of the methanesulfonates of α‐(4‐chlorophenyl)‐α‐[1‐(2‐chlorophenyl)emenyl]‐1H‐1,2,4‐triazole‐1‐ethanol and α‐[1‐(2‐chlorophenyl)ethenyl]‐α‐(2,4‐difluorophenyl)‐1H‐1,2,4‐triazole‐1‐ethanol, alpha styryl carbinol antifungal agents

Jaan A. Pesti; Jill A. Downard; Mark D. Lauritsen; Goss S. Kauffman; Walter M. Bryant; George F. Huhn; John F. Arnett; Robert E. Yule; James Segretario; Kimberly A. Nelson; Edward Gorko; Gary O. Page; Lisa M. Lloyd; Richard E. Olson; Christopher S. Bamum; Joseph J. Mrowca


Chemical Innovation | 2000

A better drug for Alzheimer's

Jaan A. Pesti; Robert J. Chorvat; George F. Huhn


Journal of Heterocyclic Chemistry | 1994

On the mechanism of the reduction of 1‐phenyl‐3‐(4‐pyridinylmethylene)‐2‐oxindole with sodium borohydride in methanol

Michael E. Pierce; George F. Huhn; James H. Jensen; Ken W. Sigvardson; Qamrul Islam; Yide Xing

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